Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15